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MX2010001677A - Derivados de 4-(9-(3,3-difluorociclopentil)-5,7,7-trimetil-6-oxo-6 ,7,8,9-tetrahidro-5h-pirimido[4,5-b][1,4]diazepin-2-ilamino)-3-me toxibenzamida como inhibidores de las proteinas cinasas humanas plk1 a plk4 para el tratamiento de enfermedades proli - Google Patents

Derivados de 4-(9-(3,3-difluorociclopentil)-5,7,7-trimetil-6-oxo-6 ,7,8,9-tetrahidro-5h-pirimido[4,5-b][1,4]diazepin-2-ilamino)-3-me toxibenzamida como inhibidores de las proteinas cinasas humanas plk1 a plk4 para el tratamiento de enfermedades proli

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Publication number
MX2010001677A
MX2010001677A MX2010001677A MX2010001677A MX2010001677A MX 2010001677 A MX2010001677 A MX 2010001677A MX 2010001677 A MX2010001677 A MX 2010001677A MX 2010001677 A MX2010001677 A MX 2010001677A MX 2010001677 A MX2010001677 A MX 2010001677A
Authority
MX
Mexico
Prior art keywords
sub
proliferative
inhibitors
protein kinases
plk1
Prior art date
Application number
MX2010001677A
Other languages
English (en)
Inventor
Jean-Damien Charrier
Francoise Pierard
Original Assignee
Vertex Pharma
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Vertex Pharma filed Critical Vertex Pharma
Publication of MX2010001677A publication Critical patent/MX2010001677A/es

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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • AHUMAN NECESSITIES
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • AHUMAN NECESSITIES
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    • A61P35/00Antineoplastic agents
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    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/14Ortho-condensed systems

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Abstract

Los compuestos de esta invención, y composiciones farmacéuticamente aceptables de los mismos, son útiles como inhibidores de proteína cinasas PK1. Estos compuestos tienen la fórmula I, como la definida en la presente o sales farmacéuticamente aceptables de los mismos. Estos compuestos y sales farmacéuticamente aceptables de los mismos, son útiles para tratar o prevenir una variedad de enfermedades, trastornos o afecciones, incluyendo, pero no limitadas a, una enfermedad autoinmune, inflamatoria, proliferativa o hiperproliferativa, una enfermedad neurodegenerativa o una enfermedad mediada inmunológicamente. Fórmula I, en donde R1 es (fórmula) ; R6 es alifático de C1-4 o cicloalifático de C3-6, y es sustituido con 1 ó 2 átomos de halógeno; X es O y R2 es CH3 o X es NR5 y R2 y R5, junto con los átomos a los cuales están unidos, forman un 1,2,4-triazol; cada uno de R3 y R4es independientemente H, metilo o etilo; o R3 y R4, junto con los átomos a los cuales están unidos, forman un anillo de ciclopropilo; y n es 0 ó 1.
MX2010001677A 2007-08-15 2008-08-15 Derivados de 4-(9-(3,3-difluorociclopentil)-5,7,7-trimetil-6-oxo-6 ,7,8,9-tetrahidro-5h-pirimido[4,5-b][1,4]diazepin-2-ilamino)-3-me toxibenzamida como inhibidores de las proteinas cinasas humanas plk1 a plk4 para el tratamiento de enfermedades proli MX2010001677A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US96482507P 2007-08-15 2007-08-15
US98062907P 2007-10-17 2007-10-17
PCT/US2008/009786 WO2009023269A2 (en) 2007-08-15 2008-08-15 4-(9-(3, 3-difluorocyclopentyl) -5, 7, 7-trimethyl-6-oxo-6, 7, 8, 9-tetrahydro-5h-pyrimido [4, 5-b[1, 4] diazepin-2-ylamino)-3-methoxybenzamide derivatives as inhibitors of the human protein kinases plk1 to plk4 for the treatment of proliferative diseases

Publications (1)

Publication Number Publication Date
MX2010001677A true MX2010001677A (es) 2010-03-11

Family

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MX2010001677A MX2010001677A (es) 2007-08-15 2008-08-15 Derivados de 4-(9-(3,3-difluorociclopentil)-5,7,7-trimetil-6-oxo-6 ,7,8,9-tetrahidro-5h-pirimido[4,5-b][1,4]diazepin-2-ilamino)-3-me toxibenzamida como inhibidores de las proteinas cinasas humanas plk1 a plk4 para el tratamiento de enfermedades proli

Country Status (9)

Country Link
US (2) US8461149B2 (es)
EP (1) EP2190849B1 (es)
JP (1) JP5380447B2 (es)
CN (1) CN101952291A (es)
AU (1) AU2008287339A1 (es)
CA (1) CA2695753A1 (es)
MX (1) MX2010001677A (es)
NZ (1) NZ583061A (es)
WO (1) WO2009023269A2 (es)

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CA2695753A1 (en) 2009-02-19
WO2009023269A3 (en) 2009-04-02
EP2190849A2 (en) 2010-06-02
JP5380447B2 (ja) 2014-01-08
US20110263575A1 (en) 2011-10-27
WO2009023269A2 (en) 2009-02-19
US20140018352A1 (en) 2014-01-16
EP2190849B1 (en) 2013-11-20
JP2010536760A (ja) 2010-12-02
US8461149B2 (en) 2013-06-11
CN101952291A (zh) 2011-01-19
AU2008287339A1 (en) 2009-02-19
NZ583061A (en) 2012-06-29

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